# Social stress and affiliative touch: A tale of two affective states

**Authors:** Lito Parapera Papantoniou, Orysia Vityk, Stamatina Tzanoulinou

PMC · DOI: 10.1016/j.isci.2026.114833 · iScience · 2026-02-02

## TL;DR

The paper explores how positive social touch and stressful social interactions affect the brain, suggesting touch could be a powerful remedy for stress.

## Contribution

The paper highlights the neural overlap in positive and negative social experiences and advocates for touch-based interventions in stress treatment.

## Key findings

- Common brain regions are involved in both positive and negative social interactions in humans and rodents.
- Affiliative touch has a buffering effect against stress and anxiety.
- More interdisciplinary research is needed to develop touch-based interventions for stress-related issues.

## Abstract

Social interactions are an integral part in the life of social species. Humans and other species, such as rats and mice, thrive on positive social interactions, whereas stressful social encounters can be among the most negative and traumatizing experiences. These traumatic experiences have often been linked to psychopathology, with some individuals being more vulnerable than others in developing maladaptations. Here, we review literature regarding both positive and negative affective states linked with prosocial/affiliative and stressful social experiences, respectively. Of all positive social interactions, social touch is a particularly potent and evolutionarily conserved behavior associated with social buffering. We examine these topics from the standpoint of both human studies and fundamental research involving rodents, as rodents are among the most commonly used model organisms. As we explore the physiological mechanisms underlying social stress and affiliative touch, our review highlights that many common brain regions are engaged in both species examined. Moreover, a substantial overlap exists in the neural substrates involved during both positive and negative social interactions. This evidence denotes the need to refine our experimental approaches to further delineate the involvement of these areas in a cell- and projection-specific manner for positive and negative social interactions. We conclude that despite the well-known buffering effects of social touch for stress and anxiety, more interdisciplinary research is needed to establish somatosensorial approaches, such as touch-based interventions, as a standard avenue in the treatment of stress-related symptomatology. We argue that social/affiliative touch could, in fact, be one of the most effective “antidotes” in the aftermath of social stress.

Neuroscience; Social sciences

## Linked entities

- **Species:** Homo sapiens (taxon 9606), Rattus norvegicus (taxon 10116), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, Hcrt (hypocretin) [NCBI Gene 15171] {aka PPOX}, Oxtr (oxytocin receptor) [NCBI Gene 18430] {aka OTR}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, Creb1 (cAMP responsive element binding protein 1) [NCBI Gene 12912] {aka 2310001E10Rik, 3526402H21Rik, Creb, Creb-1}, Gpbar1 (G protein-coupled bile acid receptor 1) [NCBI Gene 227289] {aka BG37, GPCR, GPR131, M-BAR, TGR5}, Prok2 (prokineticin 2) [NCBI Gene 50501] {aka Bv8, PK2, Prok1}, Prokr2 (prokineticin receptor 2) [NCBI Gene 246313] {aka B830005M06Rik, EG-VEGRF2, Gpcr73l1, Gpr73l1, PKR2}, Fmr1 (fragile X messenger ribonucleoprotein 1) [NCBI Gene 14265] {aka FMRP, Fmr-1}, Gpr34 (G protein-coupled receptor 34) [NCBI Gene 23890] {aka Lypsr1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, OXT (oxytocin/neurophysin I prepropeptide) [NCBI Gene 5020] {aka OT, OT-NPI, OXT-NPI}, Fosb (Fos B proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 14282], Mrgprb4 (MAS-related GPR, member B4) [NCBI Gene 233230] {aka MrgB4}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Gpr83 (G protein-coupled receptor 83) [NCBI Gene 14608] {aka Gir, Gpr72, RP105, RP39, RP82}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** intimate (MESH:C563733), deficits in cognitive processes (MESH:D003072), social anxiety disorder (MESH:D000072861), phobia (MESH:D010698), depression (MESH:D003866), chronic pain (MESH:D059350), Aggression (MESH:D010554), war (MESH:D000067398), leptin resistance (OMIM:614962), mental health disorders (OMIM:603663), stress disorders (MESH:D000079225), death (MESH:D003643), motivation deficits (MESH:D009461), MDD (MESH:D003865), decreased systolic blood pressure (MESH:D007022), CSDS (MESH:D013313), stress- and anxiety-related disorders (MESH:D001008), itch (MESH:D011537), disorders (MESH:D009358), analgesia (MESH:D000699), stress-related disorders (MESH:D000068099), mood disorders (MESH:D019964), weight gain (MESH:D015430), neglect (MESH:D058069), mental disorders (MESH:D001523), abuse (MESH:D019966), childhood maltreatment (MESH:D063766), neurotoxicity (MESH:D020258), sexual violence (MESH:D050035), bullying (MESH:D000073397), autism (MESH:D001321), anxiety (MESH:D001007), neuroinflammation (MESH:D000090862), injury (MESH:D014947), inflammation (MESH:D007249), metabolic syndrome (MESH:D024821), Pain (MESH:D010146), anhedonia (MESH:D059445), like (MESH:C537419), ASD (MESH:D000067877)
- **Chemicals:** dopamine (MESH:D004298), cannabinoid (MESH:D002186), glutamine (MESH:D005973), MDMA (MESH:D018817), ketamine (-), noradrenaline (MESH:D009638), glutamate (MESH:D018698), glycine (MESH:D005998), choline (MESH:D002794), cortisol (MESH:D006854), corticosterone (MESH:D003345), oxygen (MESH:D010100)
- **Species:** Cervus elaphus (red deer, species) [taxon 9860], Delphinidae (marine dolphins, family) [taxon 9726], Rattus norvegicus (brown rat, species) [taxon 10116], Microtus arvalis (common vole, species) [taxon 47230], Homo sapiens (human, species) [taxon 9606], Mesocricetus auratus (golden hamster, species) [taxon 10036], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12927093/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12927093/full.md

## References

312 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927093/full.md

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Source: https://tomesphere.com/paper/PMC12927093